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Not yet recruitingPhase 1

Psilocybin After Trauma Surgery for Pain

NCT07406828 · Trent Emerick

Closed to entry
Status
Not accepting participants
Phase 1
Phase
70
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

The goal of this clinical trial is to evaluate whether a single dose of psilocybin is feasible and safe for adults with opioid use disorder (OUD) who are recovering from trauma surgery. The main questions it aims to answer are: 1. Is a single psilocybin dose feasible to administer during postoperative hospitalization? 2. Is psilocybin safe in this patient population? 3. How does psilocybin affect postoperative pain, opioid use, anxiety, and depression after hospital discharge? Participants will: Receive one oral dose of psilocybin during their postoperative inpatient stay Complete assessments of pain, mood, and opioid use during recovery

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Feasibility: Recruitment

    Measured over From enrollment and receipt of psilocybin to 3 days post-treatment.

  • Feasibility: Retention

    Measured over Day 5 post-treatment

  • Feasibility: Completion of One-Month PROs

    Measured over at 1-month post-treatment

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

25 Years to 65 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: 1. ≥ 25 years old and ≤65 years old 2. Inpatient 3. English-speaking 4. History of opioid use disorder as diagnosed by DSM-V 5. Able to swallow capsules. 6. Patients are able to be enrolled and receive psilocybin within 3 days (72 hours) of surgery (time point 0 for this three-day window begins after patient arrival in the ICU) after a trauma surgery. Psilocybin will be administered in the morning to allow for the 8-hour monitoring period. Exclusion Criteria: 1. Pregnancy. Women of child-bearing potential need to have a negative pregnancy test result at screening and baseline. 2. Sexually active male participants and/or their female partners and female participants of child-bearing potential need to be on adequate and effective method of contraception (diaphragm, male condom, combined pill, copper IUD, levonorgestrel IUS, etonogestrel implant).for one week following study drug administration. 3. Breastfeeding 4. Patients receiving concurrent ketamine therapy or who have received ketamine therapy during the trauma admission. 5. UDS screen on admission (if obtained) positive for alcohol, opioids other than prescribed for pain or maintenance opioids for OUD, or other substances of abuse 6. History of psychedelic substance use in the preceding 5 years 7. History (or active) cardiovascular disease (non-optimized coronary vascular disease, stable or unstable angina, new onset EKG abnormalities, congenital long QT syndrome, cardiac trauma involving surgical repair or CABG within 1 year) 8. Screening blood pressure SBP \>140 mmHg or DBP \> 90 mmHg on three separate occasions 9. Head trauma, traumatic brain injury, or concussion. 10. Tachycardia defined as HR \> 100, averaged over the previous 12 hours, excluding intra-operative care) 11. History of dementia 12. History of pre-existing neurological conditions (including TIA, stroke, epilepsy, MS, ALS, Guillain-Barre, Parkinson's) 13. Patients on SSRIs, TCAs, MAO-Is, lithium, or other serotonergic medications, antipsychotics. Prohibited medications need to be discontinued at least 30 days prior to psilocybin dosing. 14. Patients that received intra-operative intravenous methadone dosing \> 20 mg. 15. On vasopressors 16. Hepatic impairment, mild to moderate, with Child-Pugh score ≥ 7 17. Nicotine dependence, which would prevent the patient from staying in their room for the duration of the 8-hour psilocybin study period. 18. On sedating IV infusions (propofol, ketamine, fentanyl, benzodiazepine, dexmedetomidine) 19. History of suicidal or homicidal ideations within the last year 20. History of seizure disorder 21. Requiring restraints or active sitter 22. Patients with a history of poorly controlled anxiety (GAD7 score of 10 or more), poorly controlled depression (PHQ9 score of 15 or more), panic disorder, paranoia, PTSD, bipolar disorder, any primary psychotic disorder like schizophrenia, schizoaffective disorder, or antisocial personality disorder; personal or first- or second-degree relative history of psychotic or bipolar I or II disorder 23. History of Hallucinogen Use Disorder or Hallucinogen Persisting Perception Disorder (per DSM-V) 24. Unable to consent (intubated/sedated) 25. Intellectual disability 26. Additional or anticipated surgeries within 7248 hrs of psilocybin administration 27. Discharge from hospital pending within 24 hrs of psilocybin administration 28. Any allergy to psilocybin or other inert substances in the product

Where

1 study site

FacilityCityRegionCountry
UPMC PresbyterianPittsburghPennsylvaniaUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT07406828 on ClinicalTrials.gov →

Last updated in the registry 2026-08-06. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits